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ID	DOID:0061296
PURL	http://purl.obolibrary.org/obo/DOID_0061296 Copy Copied!
Name	Meckel syndrome 11
Definition	A Meckel syndrome that has_material_basis_in homozygous mutation in the TMEM231 gene on chromosome 16q23. https://pubmed.ncbi.nlm.nih.gov/23349226/
Xrefs	MIM:615397
Parent Relationships	is_a Meckel syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance